Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 9 |
GO:0042579 | microbody | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0016020 | membrane | 2 | 3 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7WZG1
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006625 | protein targeting to peroxisome | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007031 | peroxisome organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0015919 | peroxisomal membrane transport | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016558 | protein import into peroxisome matrix | 5 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0043574 | peroxisomal transport | 4 | 1 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071806 | protein transmembrane transport | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072662 | protein localization to peroxisome | 6 | 1 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 135 | 141 | PF00089 | 0.418 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.256 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.250 |
CLV_Separin_Metazoa | 279 | 283 | PF03568 | 0.681 |
DEG_APCC_DBOX_1 | 89 | 97 | PF00400 | 0.486 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.545 |
DOC_CYCLIN_RxL_1 | 107 | 117 | PF00134 | 0.531 |
DOC_CYCLIN_RxL_1 | 144 | 157 | PF00134 | 0.343 |
DOC_MAPK_gen_1 | 145 | 154 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 216 | 224 | PF00069 | 0.544 |
DOC_PP1_RVXF_1 | 146 | 152 | PF00149 | 0.376 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.649 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 199 | 206 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 26 | 33 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 139 | 157 | PF00022 | 0.508 |
LIG_BIR_III_2 | 214 | 218 | PF00653 | 0.538 |
LIG_Clathr_ClatBox_1 | 133 | 137 | PF01394 | 0.313 |
LIG_EH1_1 | 169 | 177 | PF00400 | 0.310 |
LIG_eIF4E_1 | 170 | 176 | PF01652 | 0.388 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.570 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.582 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.651 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.723 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 70 | 78 | PF02991 | 0.360 |
LIG_LIR_LC3C_4 | 180 | 183 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.360 |
LIG_NRBOX | 92 | 98 | PF00104 | 0.341 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.449 |
LIG_SH3_1 | 79 | 85 | PF00018 | 0.531 |
LIG_SH3_2 | 85 | 90 | PF14604 | 0.531 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.531 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.298 |
LIG_UBA3_1 | 221 | 228 | PF00899 | 0.455 |
LIG_UBA3_1 | 9 | 15 | PF00899 | 0.532 |
LIG_WW_3 | 279 | 283 | PF00397 | 0.697 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.511 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.612 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.612 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.311 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.581 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.519 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.480 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.585 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.486 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.543 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.582 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.660 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.604 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.663 |
MOD_PKB_1 | 148 | 156 | PF00069 | 0.358 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.334 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.564 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.490 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.653 |
MOD_SUMO_rev_2 | 191 | 200 | PF00179 | 0.617 |
TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 147 | 150 | PF00400 | 0.336 |
TRG_NES_CRM1_1 | 123 | 137 | PF08389 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 11 | 16 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 110 | 115 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.260 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.254 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N1 | Leptomonas seymouri | 76% | 96% |
A0A0S4J0W7 | Bodo saltans | 40% | 100% |
A0A1X0NY02 | Trypanosomatidae | 52% | 96% |
A0A3R7LE72 | Trypanosoma rangeli | 47% | 100% |
A4I1S9 | Leishmania infantum | 99% | 100% |
B1AUE5 | Mus musculus | 25% | 91% |
C0HKD7 | Caenorhabditis elegans | 25% | 94% |
C9ZKD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 99% |
E9AXW3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q00940 | Pichia angusta | 25% | 100% |
Q05568 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 88% |
Q54S31 | Dictyostelium discoideum | 26% | 79% |
Q95ZB8 | Leishmania major | 95% | 100% |
V5D8I1 | Trypanosoma cruzi | 53% | 98% |